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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implant, Endosseous, Root-Form
510(k) Number K871887
Device Name ANCHOR IIA/2 STAGE OSSEO. TIT. 6/4 ALLOY IMPLANT
Applicant
Anchor Implants , Ltd.
1190 W. 8th Ave.
Vancouver, B.C.
Canada,  CA V6H 3Z4
Applicant Contact BERGMAN
Correspondent
Anchor Implants , Ltd.
1190 W. 8th Ave.
Vancouver, B.C.
Canada,  CA V6H 3Z4
Correspondent Contact BERGMAN
Regulation Number872.3640
Classification Product Code
DZE  
Date Received05/14/1987
Decision Date 07/31/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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